DOID:0110305
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autosomal dominant limb-girdle muscular dystrophy type 1
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Aliases:
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LGMD1D
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autosomal dominant limb-girdle muscular dystrophy type 1E
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muscular dystrophy limb-girdle type 1D
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muscular dystrophy limb-girdle type 1E
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Homo sapiens (human)
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DOID:0110281
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autosomal recessive limb-girdle muscular dystrophy type 2G
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Aliases:
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LGMD2G
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limb-girdle muscular dystrophy due to telethonin deficiency
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muscular dystrophy, limb-girdle, type 2G
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Homo sapiens (human)
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DOID:0110273
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autosomal dominant limb-girdle muscular dystrophy
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Homo sapiens (human)
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DOID:0110300
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obsolete autosomal dominant limb-girdle muscular dystrophy type 1A
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Homo sapiens (human)
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DOID:0110280
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autosomal recessive limb-girdle muscular dystrophy type 2F
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Aliases:
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LGMD2F
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delta-sarcoglycanopathy
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limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency
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Homo sapiens (human)
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DOID:0110306
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autosomal dominant limb-girdle muscular dystrophy type 3
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Aliases:
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LGMD1G
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autosomal dominant limb-girdle muscular dystrophy type 1G
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muscular dystrophy limb-girdle type 1G
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Homo sapiens (human)
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DOID:0110287
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autosomal recessive limb-girdle muscular dystrophy type 2S
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Aliases:
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LGMD2S
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muscular dystrophy, limb-girdle, type 2S
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Homo sapiens (human)
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DOID:0110304
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autosomal dominant limb-girdle muscular dystrophy type 2
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Aliases:
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LGMD1F
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autosomal dominant limb-girdle muscular dystrophy type 1F
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muscular dystrophy limb-girdle type 1F
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Homo sapiens (human)
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DOID:0110286
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obsolete autosomal recessive limb-girdle muscular dystrophy type 2R
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Homo sapiens (human)
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DOID:0050557
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congenital muscular dystrophy
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Homo sapiens (human)
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DOID:0080092
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myofibrillar myopathy 1
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Aliases:
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autosomal recessive limb-girdle muscular dystrophy type 2R
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desminopathy
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Homo sapiens (human)
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DOID:0060255
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rippling muscle disease 2
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Aliases:
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autosomal dominant limb-girdle muscular dystrophy type 1C
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Homo sapiens (human)
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DOID:0070247
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autosomal dominant Emery-Dreifuss muscular dystrophy 2
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Aliases:
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EDMD2
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EMD2
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Emery-Dreifuss muscular dystrophy 2, autosomal dominant
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Emery-Dreifuss muscular dystrophy, autosomal dominant
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Hauptmann-Thannhauser muscular dystrophy
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autosomal dominant limb-girdle muscular dystrophy type 1B
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muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant
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scapuloilioperoneal atrophy with cardiopathy
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Homo sapiens (human)
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DOID:0080094
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myofibrillar myopathy 3
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Aliases:
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LGMD 1A
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autosomal dominant limb-girdle muscular dystrophy type 1A
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myotilinopathy
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spheroid body myopathy
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Homo sapiens (human)
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DOID:1156
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chondrocalcinosis
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Aliases:
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calcium pyrophosphate deposition disease
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pseudogout
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Homo sapiens (human)
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DOID:17
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musculoskeletal system disease
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Homo sapiens (human)
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DOID:437
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Homo sapiens (human)
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DOID:2755
|
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Mycobacterium avium complex disease
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Aliases:
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Infection due to Mycobacterium intracellulare
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MAC disease
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Mycobacterium Avium Infection
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Mycobacterium avium Complex
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Homo sapiens (human)
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DOID:8691
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mycosis fungoides
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Aliases:
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mycosis fungoides lymphoma
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Homo sapiens (human)
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DOID:820
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|
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Homo sapiens (human)
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DOID:2661
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myoepithelioma
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Aliases:
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Myoepithelial adenoma
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Myoepithelial neoplasm
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benign myoepithelioma
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Homo sapiens (human)
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DOID:431
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|
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Homo sapiens (human)
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DOID:0080108
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|
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Homo sapiens (human)
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DOID:2691
|
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myoma
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Aliases:
-
benign neoplasm of the Muscle
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Homo sapiens (human)
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DOID:11830
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myopia
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Aliases:
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near vision
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near-sightedness
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short-sightedness
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Homo sapiens (human)
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